Canonical Allele Identifier: CA271410650

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs546466962
• gnomAD v2: 15-64449335-CAGA-C
• gnomAD v3: 15-64157136-CAGA-C
• gnomAD v4: 15-64157136-CAGA-C
• MyVariant Identifiers: chr15:g.64449336_64449338del (hg19) ; chr15:g.64157137_64157139del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157139_64157141del , CM000677.2:g.64157139_64157141del	GRCh38
NC_000015.9:g.64449338_64449340del , CM000677.1:g.64449338_64449340del	GRCh37
NC_000015.8:g.62236391_62236393del	NCBI36
NG_012979.1:g.11017_11019del , LRG_10:g.11017_11019del
NG_033071.1:g.10423_10425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-230_344-228del (PPIB) MANE Select	ENSP00000300026.4:n.344-230_344-228del
ENST00000325881.9:c.*2631_*2633del (SNX22) MANE Select	ENSP00000323435.4:n.*2631_*2633del
ENST00000561048.2:n.3341_3343del (PPIB)
ENST00000680158.1:c.*17-230_*17-228del (PPIB)	ENSP00000504873.1:n.*17-230_*17-228del
ENST00000680343.1:n.298-230_298-228del (PPIB)
ENST00000681397.1:c.344-230_344-228del (PPIB)	ENSP00000506584.1:n.344-230_344-228del
ENST00000681658.1:c.239-230_239-228del (PPIB)	ENSP00000505431.1:n.239-230_239-228del
ENST00000300026.3:c.344-230_344-228del (PPIB)	ENSP00000300026.3:n.344-230_344-228del
ENST00000325881.8:c.*2631_*2633del (SNX22)	ENSP00000323435.4:n.*2631_*2633del
ENST00000557789.5:n.3371_3373del (SNX22)
ENST00000558492.1:n.250-230_250-228del (PPIB)
ENST00000560997.1:n.3026_3028del (SNX22)
NM_000942.4:c.344-230_344-228del , LRG_10t1:c.344-230_344-228del (PPIB)	NP_000933.1:n.344-230_344-228del
NM_024798.2:c.*2631_*2633del (SNX22)	NP_079074.2:n.*2631_*2633del
NR_073534.1:n.3319_3321del (SNX22)
XM_017022581.1:c.*2631_*2633del (SNX22)	XP_016878070.1:n.*2631_*2633del
NM_024798.3:c.*2631_*2633del (SNX22) MANE Select	NP_079074.2:n.*2631_*2633del
NM_000942.5:c.344-230_344-228del (PPIB) MANE Select	NP_000933.1:n.344-230_344-228del
NR_073534.2:n.3305_3307del (SNX22)